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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

Reduced CD44 expression may cause abnormal hyaluronate buildup in cutaneous myxoma.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

The nude gene is important for skin and hair development.

Specific genes influence hair and cashmere growth in Laiwu black goats.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The Msi2 protein helps keep hair follicle stem cells inactive, controlling hair growth and regeneration.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.